39 phenotypes from 3 alleles in 5 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Plcb1em1(IMPC)Mbp/Plcb1+ C57BL/6N-Plcb1em1(IMPC)Mbp/MbpMmucd	abnormal eye morphology	J:211773
	abnormal kidney morphology	J:211773
	abnormal liver morphology	J:211773
	abnormal lymph node morphology	J:211773
	abnormal ovary morphology	J:211773
	abnormal skin morphology	J:211773
	abnormal spleen morphology	J:211773
	abnormal vitreous body morphology	J:211773
	cataract	J:211773
	enlarged kidney	J:211773
	enlarged lymph nodes	J:211773
	enlarged spleen	J:211773
	hyperactivity	J:211773
	microphthalmia	J:211773
Plcb1em1(IMPC)Mbp/Plcb1em1(IMPC)Mbp C57BL/6N-Plcb1em1(IMPC)Mbp/MbpMmucd	female infertility	J:211773
	male infertility	J:211773
Plcb1Tg(LGB)56Mbal/Plcb1Tg(LGB)56Mbal involves: C57BL/6 * CBA	abnormal brain size	J:93076
	abnormal long bone morphology	J:93076
	decreased body length	J:93076
	decreased body weight	J:93076
	disproportionate dwarf	J:93076
	enlarged cranium	J:93076
	increased cranium width	J:93076
	increased kidney weight	J:93076
	increased testis weight	J:93076
	kyphosis	J:93076
	postnatal growth retardation	J:93076
	postnatal lethality	J:93076
	reduced female fertility	J:93076
	reduced male fertility	J:93076
Plcb1tm1Hssh/Plcb1tm1Hssh involves: 129 * C57BL/6J	abnormal excitatory postsynaptic currents	J:159855
Plcb1tm1Hssh/Plcb1tm1Hssh involves: 129/Sv * C57BL/6	abnormal spatial learning	J:151070
	decreased prepulse inhibition	J:151070
	decreased startle reflex	J:151070
	hyperactivity	J:151070
Plcb1tm1Hssh/Plcb1tm1Hssh Not Specified	convulsive seizures	J:43077
	decreased body size	J:43077
	increased susceptibility to pharmacologically induced seizures	J:43077
	lethality at weaning, incomplete penetrance	J:43077
	loss of hippocampal neurons	J:43077